A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035897



Internal ID19125116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20210878..20530173hg38UCSC Ensembl
Innerchr15:20416131..20735411hg19UCSC Ensembl
Innerchr15:18676145..18995425hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38319296
hg19319281
hg18319281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2215n100
Supporting Variantsnssv3538212
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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